Sdi Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K150515 | IQSense Flow Sensor Mouthpiece | BZG | 2016-01-12 | View |
| 510(k) | K092813 | ASTRASONIC SPIROMETER, MODEL 29-8000 | BZG | 2010-07-16 | View |
| 510(k) | K061571 | ASTRA 300 | BZG | 2007-01-31 | View |
| 510(k) | K062913 | ASTRAGUARD PULMONARY FUNCTION FILTER | BZG | 2007-01-26 | View |
| 510(k) | K033939 | FLOSENSE II, MODEL 29-8040 | BZG | 2004-01-30 | View |
| 510(k) | K031643 | SPIROTEL, MODEL 29-1020 | BZG | 2003-12-09 | View |
| 510(k) | K013812 | SPIROLAB II, MODEL 29 | BZG | 2002-02-11 | View |
| 510(k) | K011470 | SDI SB OFFICE, MODEL 29- | BZG | 2001-10-12 | View |
| 510(k) | K990962 | FLOSENSE, MODEL 29-8010 | JAX | 2000-01-07 | View |
| 510(k) | K934509 | PULMOGUARD DISPOSABLE BATERIAL/VIRAL FILTER | CAH | 1993-10-21 | View |
No matching devices.
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